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Elfride De Baere | TopNews Stars
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Princess Mathilde of Belgium presents the InBev Baillet-Latour Award de la Sante to Professor Elfride De Baere at Palais des Academies on April 19, in Brussels ...
Prestigieuze Baillet Latour-prijzen uitgereikt
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De Vlaamse professor Elfride de Baere van de Universiteit van Gent krijgt dezelfde prijs voor het in kaart brengen van het nog onbekende deel ...
Physicians & MDs
Age-dependent effects of RPE65 gene therapy for Leber's congenital...
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Age-dependent effects of RPE65 gene therapy for Leber's congenital amaurosis: a phase 1 dose-escalation trial. By - Albert M Maguire MD, Prof Katherine A High...
Age-dependent effects of RPE65 gene therapy for Leber's ...
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Xiaosong Zhu, Leslie Raffini, Frauke Coppieters, Elfride De Baere, Kenneth S Shindler, Nicholas J Volpe, Enrico M Surace, Carmela Acerra,.
The Lancet : Volume 374, Number 9701, 7 November 2009
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The Lancet is the world's leading general medical journal and specialty journals in Oncology, Neurology and Infectious Diseases. Available online first. Free...
Network Profiles
LinkedIn: Elfri De Neve | LinkedIn
View Elfri De Neve’s professional profile on LinkedIn. LinkedIn is the world's largest business network, ... Elfride De Baere. Full Professor at Ghent University.
LinkedIn: Elfride De Baere | LinkedIn
View Elfride De Baere’s professional profile on LinkedIn. LinkedIn is the world's largest business network, helping professionals like Elfride De Baere discover ...
LinkedIn: Elfride De Baere - Belgium | LinkedIn
Elfride De Baere. Full Professor at Ghent University Location Gent Area, Belgium Industry Research
Interests
COST | Who's Who
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Photo Name and Position Address Phone, Fax, E-mail; Professor Elfride De Baere . Action involvement: BM Ghent Unversity Ghent University Hospital
Disruption of the Basal Body Protein POC1B Results in ...
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Elfride de Baere. Search for articles by this author, Caroline C.W. Klaver. x. Caroline C.W. Klaver. Search for articles by this author, Frauke Coppieters. x.
Sign In - The BMJ
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Elfride De Baere, Robert K Koenekoop, Rob W J Collin, Raheel Qamar, Frans P M Cremers; J Med Genet 2014; 51: Published Online First: 15 April doi: …
Mutations disrupt cellular recycling, cause a childhood genetic...
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Researchers have identified a key gene that, when mutated, causes the rare multisystem disorder Cornelia deLange syndrome. Mutations in the HDAC8 gene disrupt...
Business Profiles
Researchgate: Elfride De Baere
Gent, Belgium
Elfride De Baere - Citations - researchgate.net
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Elfride De Baere - ZoomInfo
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View Elfride De Baere's business profile as Medical Research Building at Center for Medical Genetics Ghent and see work history, affiliations and more.
Celebrities & Politicians
InBev Baillet - Latour Awards de la Sante Pictures - Zimbio
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Princess Mathilde of Belgium presents the InBev Baillet-Latour Award de la Sante to Professor Elfride De Baere at Palais des Academies on April 19, in...
Heritage
Elfride De Baere - Genealogy
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View Elfride De Baere's genealogy family tree on Geni, with over 150 million profiles of ancestors and living relatives.
Books & Literature
Gender Identity Disorder in Twins: A Review of the …
onlinelibrary.wiley.com
Gunter Heylens MD 1,*, Griet De Cuypere MD, PhD 1, Kenneth J. Zucker PhD 2, Cleo Schelfaut MD 3, Els Elaut MSc 1, Heidi Vanden Bossche MSc 4, Elfride De Baere …
Compositional biases and polyalanine runs in humans
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COCQUET, J, Elfride De Baere, S CABURET, and RA VEITIA “Compositional Biases and Polyalanine Runs in Humans.” Genetics 165 (3): 1613–1617.
Molecular Vision: Articles by the Authors
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Articles by the Authors. Articles by Julie Désir. Articles by Frauke Coppieters. Articles by Nicole Van Regemorter. Articles by Elfride De Baere
Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis...
onlinelibrary.wiley.com
Mutations in LCA5 are an uncommon cause of Leber congenital amaurosis ... an uncommon cause of Leber congenital amaurosis (LCA) type II ... , Elfride Baere, ...
Related Documents
CiteSeerX — Microarray-Based Mutation Detection and ...
citeseerx.ist.psu.edu
BibTeX @MISC{Yzer_microarray-basedmutation, author = {Suzanne Yzer and Bart P. Leroy and Elfride De Baere and Thomy J. De Ravel and Marijke N. Zonneveld and …
Age-dependent effects of RPE65 gene therapy for …
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Age-dependent eff ects of RPE65 gene therapy for Leber’s congenital amaurosis: ... Elfride De Baere, ... gene therapy for Leber's congenital amaurosis: a phase
Orphanet Journal of Rare Diseases | Abstract | Novel …
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Abstract; Full text; PDF (2.7MB) ePUB ... Thomy de Ravel 5, Elena V Semina 2 6 and Elfride De Baere 1 * ... Orphanet Journal of Rare Diseases 2014, ...
Clinical Course, Genetic Etiology, and Visual Outcome in ...
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Elfride De Baere Moll-Ramirez, Maria M. van Genderen, Camiel J.F. Boon, Arthur A.B. Bergen, Elfride De Baere, Andrew J. Lotery, and Frans P.M. Cremers.
Scientific Publications
Elfride De Baere - academic.research.microsoft.com
academic.research.microsoft.com
Elfride De Baere,Ghent University,Genetics & Genealogy,Ophthalmology,Molecular Biology. Edit Elfride De Baere
Missense mutations in the forkhead domain of FOXL2 …
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Elfride De Baere 1, * 1 Center for Medical Genetics; 2 Department of Ophthalmology, Ghent University Hospital, Ghent, Belgium 3 INSERM U567, Team
Genetic and Rare Diseases Information Center (GARD ...
rarediseases.info.nih.gov
Elfride De Baere. Blepharophimosis, Ptosis, and Epicanthus Inversus. GeneReviews. July 8, 2004; http://www.ncbi.nlm.nih.gov/books/NBK Accessed
Sarah De Jaegere - academic.research.microsoft.com
academic.research.microsoft.com
View Sarah De Jaegere's professional profile. Publications: 3 | Citations: 29 Field Rating: 3. Fields of study: Genetics & Genealogy Sign in ... Elfride De Baere. 2
Publications
Enhanced S-cone syndrome with preserved macular structure …
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Enhanced S-cone syndrome with preserved macular structure ... Enhanced S-cone syndrome with preserved macular structure and severely depressed ... Elfride De Baere
FOXL2 mutations in Indian families with blepharophimosis ...
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Elfride De Baere (4) Periasamy Sundaresan (1) Author Affiliations. 1. Department of Genetics, Dr. G. Venkataswamy Eye Research Institute, Aravind Medical Research ...
Publications Authored by Elfride De Baere
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Publications Authored By Elfride De Baere Nov. De novo MECP2 duplications in two females with intellectual disability and unfavorable complete skewed ...
SpringerCitations - Details Page
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Ivan Cima, Jelka Brecelj, Maja Sustar, Frauke Coppieters, Bart P. Leroy, Elfride Baere and Marko Hawlina. Journal: Documenta Ophthalmologica, 2012, Volume ...
Reports & Statements
nature.com search
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& Elfride De Baere. Genetics in Medicine 16, 671–680. Rights & permissions Opens in a new window. Research | 26 January Massively parallel sequencing for ...
Twitter Posts: FWO auf Twitter: "Elfride De Baere (UGent) wint de InBev-Baillet...
Elfride De Baere (UGent) wint de InBev-Baillet Latour Prijs voor Klinisch Onderzoek #FWOFlanders #ugent http://bit.ly/JcGt7Q.
Wikipedia: Blefarofimosi - Wikipedia
Elfride De Baere, Blepharophimosis, Ptosis, and Epicanthus Inversus, University of Washington, Seattle, Pagon RA, Adam MP, Bird TD, et al., editors.
Elfride De Baere is de nieuwe blogger van de week. Lees haar bijdrage...
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Elfride De Baere is de nieuwe blogger van de week. Lees haar bijdrage via http://www.durfdenken.be/blog/os ugent-goes-olympic
Miscellaneous
Elfride De Baere | Center for Medical Genetics
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Contact. Center for Medical Genetics Ghent University Hospital De Pintelaan 185, Ghent Belgium. Tel. + Fax. +
Contribution of growth differentiation factor 6-dependent …
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... Irma Lopez, Curtis R French, Jakub Famulski, Elfride De Baere, Peter J Francis, Periasamy Sundaresan, Yves Sauvé, Robert K Koenekoop, Fred B Berry, ...
FOXL2 Impairment in Human Disease - Karger …
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FOXL2 Impairment in Human Disease Hannah Verdin Elfride De Baere Center for Medical Genetics, Ghent University Hospital, Ghent , Belgium
Genetic Testing - Mary Ann Liebert, Inc. publishers
online.liebertpub.com
Genetic Testing. December 2001, 5(4): doi: Elfride De Baere, Diane Beysen, Christine Oley, ...
IOVS | Molecular Diagnosis Of Autosomal Recessive …
iovs.arvojournals.org
Molecular Diagnosis Of Autosomal Recessive Retinal Dystrophies By Homozygosity ... Elfride De Baere, ... Of Autosomal Recessive Retinal Dystrophies By ...
International Journal of Research in Medical Sciences
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Elfride De Baere. Blepharophimosis, Ptosis and Epicanthus Inversus. In: Pagon RA, Bird TD, Dolan CR, ... doi: ijrms Web Style. Abhilash K.
Lab De Baere | Centrum Medische Genetica
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Lab De Baere. Lab De Baere. Research topics . Developmental genetics. CIS-CODE: ... Elfride De Baere. Postdoctoral researchers . Hannah Verdin. PhD students . …
Reproduction Nutrition Development
rnd.edpsciences.org
Reproduction Nutrition Development, ... Edmond Cribiu c, Elfride De Baere e, Yann Guiguen a, Francis Jaubert b, Eric Pailhoux d, Maëlle Pannetier d, ...
The Inbev-Baillet Latour Fund awards the prize for ...
www.vision-research.eu
Professor Elfride De Baere, recipient of the InBev-Baillet Latour Prize for Clinical Research Professor Elfride De Baere.
erdc | Partners
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Prof. dr. Elfride de Baere. Dr. Frauke Coppieters Consortium Partners . ERDC consists of 15 research groups, 13 from Europe, one from Canada, and one from the …
FOXL2 mutations in Indian families with blepharophimosis ...
www.infona.pl
Elfride Baere. Ghent University Hospital, Center for Medical Genetics, Ghent, Belgium; Periasamy Sundaresan. Aravind Medical Research Foundation, Department of ...
Elfride De Baere - Cites de Google Acadèmic
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Cites combinades. La llista anomenada Citats per inclou les cites als articles següents de Google Acadèmic. Els articles marcats amb una * poden ser diferents ...
Bérénice A. Benayoun - Google 学术搜索引用
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... Jana P. Lim,; jeyabalan nallathambi,; Elfride De Baere,; Vaiman Daniel,; Yevgeniy Izrayelit,; Frank C Schroeder,; Aaron C. Daugherty,; Keerthana Devarajan, ...
Elfride De Baere krijgt prestigieuze Inbev-Baillet-Latour Prijs voor...
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23 Apr 2012, Posted by Ann in Blog,Slider,Voorpagina, No Comments. Elfride De Baere krijgt prestigieuze Inbev-Baillet-Latour Prijs voor Klinisch Onderzoek 2012
UZ Gent - Elfride De Baere krijgt prestigieuze Inbev-Baillet-Latour...
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Prof. dr. Elfride De Baere wordt gelauwerd voor haar baanbrekend onderzoekswerk in medische genetica, meer bepaald voor het in kaart brengen van het nog
Elfride De Baere
biblio.ugent.be
Elfride De Baere Barbara D'haene UGent, Elfride De Baere UGent, Hannah Verdin UGent, Pino J Poddighe, Robert-Jan Galjaard and Joost Gribnau, et al.
Orphanet: Dr Elfride DE BAERE
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Le portail des maladies rares et des médicaments orphelins
Elfride De Baere | Centrum Medische Genetica
cmgg.be
Positional cloning, candidate gene aproach and mutation analysis in the blepharophimosis syndrome. Year: Internal supervisor(s): Anne De Paepe.
Novel insights into the molecular pathogenesis of CYP4V2 -associated...
www.academia.edu
By Ulrich Kellner and Bernhard Jurklies.
Enhanced S-cone syndrome with preserved macular structure and...
www.infona.pl
... macular structure and severely depressed retinal function. Ivan Cima, Jelka Brecelj, Maja Sustar, Frauke Coppieters, Bart Leroy, Elfride Baere, Marko Hawlina.
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